Boodhansingh, K. E., Kandasamy, B., Mitteer, L., Givler, S., De Leon, D. D., Shyng, S., . . . Stanley, C. A. (2019). Novel dominant K(ATP) channel mutations in infants with congenital hyperinsulinism: Validation by in vitro expression studies and in vivo carrier phenotyping. Am J Med Genet A.
Citación estilo ChicagoBoodhansingh, Kara E., Balamurugan Kandasamy, Lauren Mitteer, Stephanie Givler, Diva D. De Leon, Show‐Ling Shyng, Arupa Ganguly, and Charles A. Stanley. "Novel Dominant K(ATP) Channel Mutations in Infants With Congenital Hyperinsulinism: Validation By in Vitro Expression Studies and in Vivo Carrier Phenotyping." Am J Med Genet A 2019.
Cita MLABoodhansingh, Kara E., et al. "Novel Dominant K(ATP) Channel Mutations in Infants With Congenital Hyperinsulinism: Validation By in Vitro Expression Studies and in Vivo Carrier Phenotyping." Am J Med Genet A 2019.